A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6112258



Internal ID22021493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1894043..1939857hg38UCSC Ensembl
chr11:1915273..1961087hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3845815
hg1945815
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17578831
Samples
Known GenesTNNT3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6112258
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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